
doi: 10.1246/bcsj.57.603
Abstract The ozonation of xanthene was studied using an oxygen stream. Ozone attacks the methylene group of xanthene via a 1,3-dipolar insertion reaction to give the hydrotrioxide intermediate, followed by a loss of singlet oxygen to form xanthydrol. The ozonation of xanthydrol gave singlet oxygen, water and xanthone accompanied by autoxidation.
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